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Global Regulatory Affairs Manager - Biocides (all genders)

Your tasks

As a Global Regulatory Affairs Manager you are responsible for the authorization of biocidal products and other regulatory activities under the regime of the EU BPR but also including comparable jurisdictions in other target markets (e.g. US FIFRA, K-BPR). You assess the respective country specific regulatory status, develop registration strategies, support active substance registration dossiers to enable compliant import, production, marketability and safe use of Life Science products. You are delighted to solve the toughest problems in our exciting and fast-growing Life Science business in the area of Regulatory Affairs based on in-depth industry knowledge and sound Regulatory Affairs expertise. In your day-to-day business you work on the registration/authorization of biocidal products under several national legislations within cross-functional, international teams. Furthermore, you act as an advisor and Regulatory Affairs representative for the “biocides management” in cross-functional teams.


Who you are

  • Graduate degree in Natural Sciences (e.g. biologist, chemist), higher degree preferable (e.g. PhD)
  • Min. 3 years of profound experience and expertise in the area of biocides regulations
  • Excellent interpersonal/intercultural skills
  • Very good project management, analytical and IT skills
  • Excellent communication skills (very good command of English; German will be an advantage), personally and through high quality documentation (presentations, reports, charts, etc.)
Job Requisition ID:  188465
Location:  Darmstadt
Career Level:  C - Professional (1-3 years)
Working time model:  full-time

Job Segment: Medical, Manager, Project Manager, Healthcare, Management, Technology

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